Organ complications after CD19 CAR T-cell therapy for large B cell lymphoma: a retrospective study from the EBMT transplant complications and lymphoma working party
We investigated >= grade 3 (CTC-AE) organ toxicities for commercial CD19 chimeric antigen receptor T cell (CAR-T cell) products in 492 patients (Axi-Cel; n = 315; Tisa-Cel; n = 177) with Large B-cell Lymphoma in the European Society for Blood and Marrow Transplantation (EBMT) CAR-T registry. The...
| Authors: | , , , , , , , , , , , , , , , , , , , , , , , |
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| Format: | article |
| Status: | Published version |
| Publication Date: | 2023 |
| Country: | España |
| Institution: | Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya) |
| Repository: | Recercat. Dipósit de la Recerca de Catalunya |
| OAI Identifier: | oai:recercat.cat:2445/208421 |
| Online Access: | https://hdl.handle.net/2445/208421 |
| Access Level: | Open access |
| Keyword: | Limfomes Receptors cel·lulars Lymphomas Cell receptors |
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Organ complications after CD19 CAR T-cell therapy for large B cell lymphoma: a retrospective study from the EBMT transplant complications and lymphoma working partyPenack, OlafPeczynski, ChristopheKoenecke, ChristianPolge, EmmanuelleSanderson, RobinYakoub Agha, IbrahimFegueux, NathalieDaskalakis, MichaelCollin, MatthewDreger, PeterKröger, NicolausSchanz, UrsBloor, AdrianGanser, ArnoldBesley, CarolineWulf, Gerald G.Novak, UrbanMoiseev, IvanSchoemans, HélèneBasak, Grzegorz W.Chabannon, ChristianSureda, AnnaGlass, BertramPeric, ZinaidaLimfomesReceptors cel·lularsLymphomasCell receptorsWe investigated >= grade 3 (CTC-AE) organ toxicities for commercial CD19 chimeric antigen receptor T cell (CAR-T cell) products in 492 patients (Axi-Cel; n = 315; Tisa-Cel; n = 177) with Large B-cell Lymphoma in the European Society for Blood and Marrow Transplantation (EBMT) CAR-T registry. The incidence of >= grade 3 organ toxicities during the first 100 days after CAR-T was low and the most frequent were: renal (3.0%), cardiac (2.3%), gastro-intestinal (2.3%) and hepatic (1.8%). The majority occurred within three weeks after CAR-T cell therapy. Overall survival was 83.1% [79.8-86.5; 95% CI] at 3 months and 53.5% [49-58.4; 95% CI] at one year after CAR-T. The most frequent cause of death was tumour progression (85.1%). Non-relapse mortality was 3.1% [2.3-4.1; 95% CI] at 3 months and 5.2% [4.1-6.5; 95% CI] at one year after CAR-T. The most frequent causes of non-relapse mortality were cell-therapy-related toxicities including organ toxicities (6.4% of total deaths) and infections (4.4% of total deaths). Our data demonstrates good safety in the European real-world setting.Frontiers Media SA2024202420232023info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersion10 p.application/pdfhttps://hdl.handle.net/2445/208421Articles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL))reponame:Recercat. Dipósit de la Recerca de Catalunyainstname:Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya)InglésReproducció del document publicat a: https://doi.org/10.3389/fimmu.2023.1252811Frontiers in Immunology, 2023, vol. 14https://doi.org/10.3389/fimmu.2023.1252811cc by (c) Penack, Olaf et al., 2023http://creativecommons.org/licenses/by/3.0/es/info:eu-repo/semantics/openAccessoai:recercat.cat:2445/2084212026-05-29T05:05:01Z |
| dc.title.none.fl_str_mv |
Organ complications after CD19 CAR T-cell therapy for large B cell lymphoma: a retrospective study from the EBMT transplant complications and lymphoma working party |
| title |
Organ complications after CD19 CAR T-cell therapy for large B cell lymphoma: a retrospective study from the EBMT transplant complications and lymphoma working party |
| spellingShingle |
Organ complications after CD19 CAR T-cell therapy for large B cell lymphoma: a retrospective study from the EBMT transplant complications and lymphoma working party Penack, Olaf Limfomes Receptors cel·lulars Lymphomas Cell receptors |
| title_short |
Organ complications after CD19 CAR T-cell therapy for large B cell lymphoma: a retrospective study from the EBMT transplant complications and lymphoma working party |
| title_full |
Organ complications after CD19 CAR T-cell therapy for large B cell lymphoma: a retrospective study from the EBMT transplant complications and lymphoma working party |
| title_fullStr |
Organ complications after CD19 CAR T-cell therapy for large B cell lymphoma: a retrospective study from the EBMT transplant complications and lymphoma working party |
| title_full_unstemmed |
Organ complications after CD19 CAR T-cell therapy for large B cell lymphoma: a retrospective study from the EBMT transplant complications and lymphoma working party |
| title_sort |
Organ complications after CD19 CAR T-cell therapy for large B cell lymphoma: a retrospective study from the EBMT transplant complications and lymphoma working party |
| dc.creator.none.fl_str_mv |
Penack, Olaf Peczynski, Christophe Koenecke, Christian Polge, Emmanuelle Sanderson, Robin Yakoub Agha, Ibrahim Fegueux, Nathalie Daskalakis, Michael Collin, Matthew Dreger, Peter Kröger, Nicolaus Schanz, Urs Bloor, Adrian Ganser, Arnold Besley, Caroline Wulf, Gerald G. Novak, Urban Moiseev, Ivan Schoemans, Hélène Basak, Grzegorz W. Chabannon, Christian Sureda, Anna Glass, Bertram Peric, Zinaida |
| author |
Penack, Olaf |
| author_facet |
Penack, Olaf Peczynski, Christophe Koenecke, Christian Polge, Emmanuelle Sanderson, Robin Yakoub Agha, Ibrahim Fegueux, Nathalie Daskalakis, Michael Collin, Matthew Dreger, Peter Kröger, Nicolaus Schanz, Urs Bloor, Adrian Ganser, Arnold Besley, Caroline Wulf, Gerald G. Novak, Urban Moiseev, Ivan Schoemans, Hélène Basak, Grzegorz W. Chabannon, Christian Sureda, Anna Glass, Bertram Peric, Zinaida |
| author_role |
author |
| author2 |
Peczynski, Christophe Koenecke, Christian Polge, Emmanuelle Sanderson, Robin Yakoub Agha, Ibrahim Fegueux, Nathalie Daskalakis, Michael Collin, Matthew Dreger, Peter Kröger, Nicolaus Schanz, Urs Bloor, Adrian Ganser, Arnold Besley, Caroline Wulf, Gerald G. Novak, Urban Moiseev, Ivan Schoemans, Hélène Basak, Grzegorz W. Chabannon, Christian Sureda, Anna Glass, Bertram Peric, Zinaida |
| author2_role |
author author author author author author author author author author author author author author author author author author author author author author author |
| dc.subject.none.fl_str_mv |
Limfomes Receptors cel·lulars Lymphomas Cell receptors |
| topic |
Limfomes Receptors cel·lulars Lymphomas Cell receptors |
| description |
We investigated >= grade 3 (CTC-AE) organ toxicities for commercial CD19 chimeric antigen receptor T cell (CAR-T cell) products in 492 patients (Axi-Cel; n = 315; Tisa-Cel; n = 177) with Large B-cell Lymphoma in the European Society for Blood and Marrow Transplantation (EBMT) CAR-T registry. The incidence of >= grade 3 organ toxicities during the first 100 days after CAR-T was low and the most frequent were: renal (3.0%), cardiac (2.3%), gastro-intestinal (2.3%) and hepatic (1.8%). The majority occurred within three weeks after CAR-T cell therapy. Overall survival was 83.1% [79.8-86.5; 95% CI] at 3 months and 53.5% [49-58.4; 95% CI] at one year after CAR-T. The most frequent cause of death was tumour progression (85.1%). Non-relapse mortality was 3.1% [2.3-4.1; 95% CI] at 3 months and 5.2% [4.1-6.5; 95% CI] at one year after CAR-T. The most frequent causes of non-relapse mortality were cell-therapy-related toxicities including organ toxicities (6.4% of total deaths) and infections (4.4% of total deaths). Our data demonstrates good safety in the European real-world setting. |
| publishDate |
2023 |
| dc.date.none.fl_str_mv |
2023 2023 2024 2024 |
| dc.type.none.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion |
| format |
article |
| status_str |
publishedVersion |
| dc.identifier.none.fl_str_mv |
https://hdl.handle.net/2445/208421 |
| url |
https://hdl.handle.net/2445/208421 |
| dc.language.none.fl_str_mv |
Inglés |
| language_invalid_str_mv |
Inglés |
| dc.relation.none.fl_str_mv |
Reproducció del document publicat a: https://doi.org/10.3389/fimmu.2023.1252811 Frontiers in Immunology, 2023, vol. 14 https://doi.org/10.3389/fimmu.2023.1252811 |
| dc.rights.none.fl_str_mv |
cc by (c) Penack, Olaf et al., 2023 http://creativecommons.org/licenses/by/3.0/es/ info:eu-repo/semantics/openAccess |
| rights_invalid_str_mv |
cc by (c) Penack, Olaf et al., 2023 http://creativecommons.org/licenses/by/3.0/es/ |
| eu_rights_str_mv |
openAccess |
| dc.format.none.fl_str_mv |
10 p. application/pdf |
| dc.publisher.none.fl_str_mv |
Frontiers Media SA |
| publisher.none.fl_str_mv |
Frontiers Media SA |
| dc.source.none.fl_str_mv |
Articles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL)) reponame:Recercat. Dipósit de la Recerca de Catalunya instname:Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya) |
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Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya) |
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Recercat. Dipósit de la Recerca de Catalunya |
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Recercat. Dipósit de la Recerca de Catalunya |
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